Syncor Intl. Corp.
Mchenry, IL, US
Syncor Intl. Corp. appears in FDA device records in Mchenry, IL. FDA records list 31 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 31
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 31 510(k) clearances for Syncor Intl. Corp. between 1983 and 1995. The busiest year on record is 1984, with 17. The most recent is 1995, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 1 |
| 1984 | 17 |
| 1985 | 12 |
| 1995 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K945825 | SECURE SAFETY INSERT | FMI | Substantially Equivalent | |
| K851828 | IRRADIATOR FOR BIOLOGICAL MATERIALS IBL-437-C | MOT | Substantially Equivalent | |
| K852023 | CESIUM 137 SOURCE, CSM-4, CSM-11, CSM-41 | KXK | Substantially Equivalent | |
| K850433 | CESIUM 137 ENDOMETRIAL SOURCE | KXK | Substantially Equivalent | |
| K852665 | SYNCOR TRICH DIRECT IMMUNOFLUORESCENCE ASSAY | JWZ | Substantially Equivalent | |
| K851033 | SYNCORTECH CHLAMYDIA DIRECT SPECIMAN KIT | LJP | Substantially Equivalent | |
| K844735 | PTH-RIA | CEW | Substantially Equivalent | |
| K850726 | WIRE CUTTERS, BRACHYTHERAPY-TABLE TOP & HAND HELD | IWA | Substantially Equivalent | |
| K850434 | CS137 SEALED SOURCES | KXK | Substantially Equivalent | |
| K850208 | FLOOD SOURCES & DOSE CALIBRATORS W/VARIOUS NUCLIDS | IXD | Substantially Equivalent | |
| K850163 | IRIDIUM 192 WIRES | IWA | Substantially Equivalent | |
| K850207 | PENPOINT, FLEXIBLE & SPOT MARKERS & RADOACTIVE RUL | Substantially Equivalent | ||
| K844582 | SYNCOR TECH CHLAMYDIA TISSUE CULTURE TEST | LJP | Substantially Equivalent | |
| K844160 | VENTIBOX | KPY | Substantially Equivalent | |
| K844181 | ACTH RIA | CKG | Substantially Equivalent | |
| K842445 | LH RIA | CEP | Substantially Equivalent | |
| K842444 | FSH RIA | CGJ | Substantially Equivalent | |
| K842598 | STAR HCG MONOCLONAL ANTIBODY IMMUNO | JHI | Substantially Equivalent | |
| K842167 | TBG RIA | CEE | Substantially Equivalent | |
| K841963 | GASTRIN RIA | CGC | Substantially Equivalent | |
| K841927 | T3 UPTAKE | KHQ | Substantially Equivalent | |
| K841854 | BHCG RIA | JHI | Substantially Equivalent | |
| K840127 | CURIETRON | JAQ | Substantially Equivalent | |
| K833851 | HCG RIA | JHI | Substantially Equivalent | |
| K833853 | T3 RIA | CDP | Substantially Equivalent | |
| K833849 | ACTH RIA | CKG | Substantially Equivalent | |
| K832796 | STAR HCG MONOCLONAL ANTIBODY IMMUNORAD | JHI | Substantially Equivalent | |
| K833850 | T4 RIA | CDX | Substantially Equivalent | |
| K833854 | LH RIA | CEP | Substantially Equivalent | |
| K833852 | FSH RIA | CGJ | Substantially Equivalent | |
| K833910 | TSH RIA | ETD | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- LJPAntiserum, Fluorescent, Chlamydia Trachomatis
- MOTIrradiator, Blood To Prevent Graft Versus Host Disease
- JWZKit, Screening, Trichomonas
- FMINeedle, Hypodermic, Single Lumen
- KHQRadioassay, Triiodothyronine Uptake
- CKGRadioimmunoassay, Acth
- CGJRadioimmunoassay, Follicle-Stimulating Hormone
- CGCRadioimmunoassay, Gastrin
- CEPRadioimmunoassay, Luteinizing Hormone
- CEWRadioimmunoassay, Parathyroid Hormone
- CEERadioimmunoassay, Thyroxine-Binding Globulin
- CDXRadioimmunoassay, Total Thyroxine
- CDPRadioimmunoassay, Total Triiodothyronine
- KPYShield, Protective, Personnel
- KXKSource, Brachytherapy, Radionuclide
- IXDSource, Calibration, Sealed, Nuclear
- IWASource, Wire, Iridium, Radioactive
- JAQSystem, Applicator, Radionuclide, Remote-Controlled
- ETDTube, Tympanostomy
- JHIVisual, Pregnancy Hcg, Prescription Use
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain